Works matching IS 13518216 AND DT 2015 AND VI 21 AND IP 5
Results: 45
A longitudinal evaluation of anti- FVIII antibodies demonstrated IgG4 subclass is mainly correlated with high-titre inhibitor in haemophilia A patients.
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- Haemophilia, 2015, v. 21, n. 5, p. 686, doi. 10.1111/hae.12646
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Deep venous thrombosis was not detected after total knee arthroplasty in Japanese patients with haemophilia.
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- Haemophilia, 2015, v. 21, n. 5, p. 585, doi. 10.1111/hae.12643
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The molecular basis of low activity levels of coagulation factor VII: a Brazilian cohort.
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- Haemophilia, 2015, v. 21, n. 5, p. 670, doi. 10.1111/hae.12645
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In silico analyses of missense mutations in coagulation factor VIII: identification of severity determinants of haemophilia A.
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- Haemophilia, 2015, v. 21, n. 5, p. 662, doi. 10.1111/hae.12662
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Delayed recurrent bleeding from central venous catheter track after catheter removal in a haemophilia patient.
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- Haemophilia, 2015, v. 21, n. 5, p. e411, doi. 10.1111/hae.12540
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Computational prediction of phenotype in haemophilia A.
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- Haemophilia, 2015, v. 21, n. 5, p. 659, doi. 10.1111/hae.12694
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Response to Croteau & Neufeld Editorial: 'Transition considerations for extended half-life factor products'.
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- Haemophilia, 2015, v. 21, n. 5, p. e451, doi. 10.1111/hae.12695
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Interpreting important health-related quality of life change using the Haem-A-QoL.
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- Haemophilia, 2015, v. 21, n. 5, p. 578, doi. 10.1111/hae.12642
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The Platelet Function Analyser ( PFA)-100 and von Willebrand disease: a story well over 16 years in the making.
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- Haemophilia, 2015, v. 21, n. 5, p. 642, doi. 10.1111/hae.12710
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US Guidelines for immune tolerance induction in patients with haemophilia a and inhibitors.
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- Haemophilia, 2015, v. 21, n. 5, p. 559, doi. 10.1111/hae.12730
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Clinical phenotype in genetically confirmed von Willebrand disease type 2N patients reflects a haemophilia A phenotype.
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- Haemophilia, 2015, v. 21, n. 5, p. e375, doi. 10.1111/hae.12733
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Venous thrombosis in afibrinogenemia: a successful use of rivaroxaban.
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- Haemophilia, 2015, v. 21, n. 5, p. e431, doi. 10.1111/hae.12734
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Low mortality from intracranial haemorrhage in paediatric patients with haemophilia.
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- Haemophilia, 2015, v. 21, n. 5, p. e359, doi. 10.1111/hae.12716
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Author's response: 'Transition considerations for extended half-life factor products'.
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- Haemophilia, 2015, v. 21, n. 5, p. e454, doi. 10.1111/hae.12718
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- Article
Management of pregnancy in type 3 von Willebrand disease with additional platelet dysfunction.
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- Haemophilia, 2015, v. 21, n. 5, p. e412, doi. 10.1111/hae.12598
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Unravelling adherence to prophylaxis in haemophilia: a patients' perspective.
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- Haemophilia, 2015, v. 21, n. 5, p. 612, doi. 10.1111/hae.12660
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The first report of a multi-exon duplication in the F9 gene causative of severe haemophilia B.
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- Haemophilia, 2015, v. 21, n. 5, p. e433, doi. 10.1111/hae.12735
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Changes in von Willebrand factor level and von Willebrand activity with age in type 1 von Willebrand disease.
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- Haemophilia, 2015, v. 21, n. 5, p. 636, doi. 10.1111/hae.12664
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The EPIC study: a lesson to learn.
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- Haemophilia, 2015, v. 21, n. 5, p. 622, doi. 10.1111/hae.12666
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- Article
Factor levels in carriers of haemophilia are associated with familial severity: a Danish single centre study.
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- Haemophilia, 2015, v. 21, n. 5, p. e440, doi. 10.1111/hae.12738
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- Article
Platelet function analyser ( PFA-100) results and von Willebrand factor deficiency: a 16-year 'real-world' experience.
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- Haemophilia, 2015, v. 21, n. 5, p. 646, doi. 10.1111/hae.12653
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Long-term patterns of safety and efficacy of bleeding prophylaxis with turoctocog alfa (NovoEight<sup>®</sup>) in previously treated patients with severe haemophilia A: interim results of the guardian<sup>™</sup>2 extension trial.
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- Haemophilia, 2015, v. 21, n. 5, p. e436, doi. 10.1111/hae.12737
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Factors influencing illness representations and perceived adherence in haemophilic patients: a pilot study.
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- Haemophilia, 2015, v. 21, n. 5, p. 598, doi. 10.1111/hae.12654
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Disclosing haemophilia at school: strategies employed by mothers of children with haemophilia in Japan.
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- Haemophilia, 2015, v. 21, n. 5, p. 629, doi. 10.1111/hae.12674
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Bone health in persons with haemophilia.
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- Haemophilia, 2015, v. 21, n. 5, p. 568, doi. 10.1111/hae.12736
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Total ankle replacement in patients with von Willebrand disease: mid-term results of 18 procedures.
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- Haemophilia, 2015, v. 21, n. 5, p. e389, doi. 10.1111/hae.12561
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Management of adult non-severe haemophilia A patients with inhibitors: a practice-pattern survey.
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- Haemophilia, 2015, v. 21, n. 5, p. e422, doi. 10.1111/hae.12727
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Postpartum haemorrhage in women with von Willebrand disease: an observational study of the Pennsylvania Health Care Cost Containment Council (PHC4) database.
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- Haemophilia, 2015, v. 21, n. 5, p. e442, doi. 10.1111/hae.12739
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Health-related quality of life assessment in haemophilia patients on prophylaxis therapy: a systematic review of results from prospective clinical trials.
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- Haemophilia, 2015, v. 21, n. 5, p. e344, doi. 10.1111/hae.12759
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Haemophilia pseudotumours in patients with inhibitors.
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- Haemophilia, 2015, v. 21, n. 5, p. 681, doi. 10.1111/hae.12632
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Acute effects of exercise on specific and global coagulation parameters in severe haemophilia A.
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- Haemophilia, 2015, v. 21, n. 5, p. e416, doi. 10.1111/hae.12700
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Presentation and management of acute coronary syndromes among adult persons with haemophilia: results of an international, retrospective, 10-year survey.
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- Haemophilia, 2015, v. 21, n. 5, p. 589, doi. 10.1111/hae.12652
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Haemophilia care in Central and Eastern Europe: challenges and ways forward from clinicians' perspective.
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- Haemophilia, 2015, v. 21, n. 5, p. e419, doi. 10.1111/hae.12706
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Oral health status in children and adolescents with haemophilia.
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- Haemophilia, 2015, v. 21, n. 5, p. 605, doi. 10.1111/hae.12657
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The use of short-term central venous catheters for optimizing continuous infusion of coagulation factor concentrate in haemophilia patients undergoing major surgical procedures.
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- Haemophilia, 2015, v. 21, n. 5, p. e364, doi. 10.1111/hae.12722
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Experimental study on the role of intra-articular injection of MSCs on cartilage regeneration in haemophilia.
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- Haemophilia, 2015, v. 21, n. 5, p. 693, doi. 10.1111/hae.12659
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The features of clearance in recombinant factor IX (BeneFIX<sup>®</sup>).
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- Haemophilia, 2015, v. 21, n. 5, p. 702, doi. 10.1111/hae.12672
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Switching to low dose of plasma-derived factor VIII/ vWF concentrates with Confact<sup>®</sup>-F as salvage immune tolerance induction in haemophilia A patients with inhibitors: five case reports from Japan.
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- Haemophilia, 2015, v. 21, n. 5, p. e425, doi. 10.1111/hae.12728
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A comprehensive study of current haemophilia care and outcomes in Singapore.
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- Haemophilia, 2015, v. 21, n. 5, p. e428, doi. 10.1111/hae.12729
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Central venous access device (CVAD) complications in Haemophilia with inhibitors undergoing immune tolerance induction: Lessons from the international immune tolerance study.
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- Haemophilia, 2015, v. 21, n. 5, p. e369, doi. 10.1111/hae.12740
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Clinical features of 32 new Japanese cases with autoimmune haemorrha-philia.
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- Haemophilia, 2015, v. 21, n. 5, p. 653, doi. 10.1111/hae.12677
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Management strategies in patients with diffuse large B-cell lymphoma and severe haemophilia.
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- Haemophilia, 2015, v. 21, n. 5, p. e445, doi. 10.1111/hae.12741
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Heterogeneity of information regarding inhibitors in the product monographs of antihaemophilic factors in North America.
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- Haemophilia, 2015, v. 21, n. 5, p. e448, doi. 10.1111/hae.12742
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Longitudinal assessment of bone loss using quantitative ultrasound in a blood-induced arthritis rabbit model.
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- Haemophilia, 2015, v. 21, n. 5, p. e402, doi. 10.1111/hae.12743
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Generation and optimization of the self-administered bleeding assessment tool and its validation as a screening test for von Willebrand disease.
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- Haemophilia, 2015, v. 21, n. 5, p. e384, doi. 10.1111/hae.12747
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